Variant #0001037104 (NC_000009.11:g.100819182del, NM_018946.3:c.92del (NANS))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.100819182del
DNA change (hg38) -
Published as NANS(NM_018946.3):c.92delG (p.G31Afs*5), NANS(NM_018946.4):c.92del (p.(Gly31Alafs*5))
ISCN -
DB-ID NANS_000001 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRIM14 NM_014788.2 +?/. - c.*30572del r.(?) p.(=)
NANS NM_018946.3 +?/. - c.92del r.(?) p.(Gly31AlafsTer5)


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